Manipulatable delivery catheter for occlusive devices (II)

ABSTRACT

This is in the general field of surgical instruments and is specifically a delivery catheter with a flexible, proximally-manipulated hinge or joint region. The inventive catheter may have a balloon region. The catheter may have a shaft of varying flexibility which contains several lumen. The inner, or delivery, lumen generally may be used with a guidewire to access target sites within the body via the flexible, small diameter vessels of the body. The delivery lumen may be also used for placement of occlusive materials, e.g., in an aneurysm. Inflation of the micro-balloon, located near the distal tip of the catheter, is effected using the inflation lumen. The push/pull wire lumen contains a wire, which when manipulated, flexes the catheter&#39;s distal tip. The push/pull wire tubing may have a variable thickness to aid in adjusting the degree of flexibility. Moreover, the delivery catheter may be capable of twisting in a helical or corkscrew-like manner for traversing certain vasculature. This may be accomplished by winding the push/pull wire within the catheter and fixedly attaching it. The catheter may further include an entry in the catheter wall to allow for the insertion of a guidewire; this may facilitate the rapid exchange of catheter devices as desired by the user.

RELATED APPLICATIONS

This is a divisional of U.S. patent application Ser. No. 09/703,468filed Oct. 31, 2000 now U.S. Pat. No. 6,482,221 entitled “MANIPULATABLEDELIVERY CATHETER FOR OCCLUSIVE DEVICES (II)”, which is acontinuation-in-part of U.S. patent application Ser. No. 09/643,085entitled “MANIPULATABLE DELIVERY CATHETER FOR OCCLUSIVE DEVICES” filedAug. 21, 2000, now U.S. Pat. No. 6,726,700 and incorporated by referencein its entirety.

FIELD OF THE INVENTION

This invention is in the general field of surgical instruments and isspecifically a catheter having a flexible, proximally-manipulated hingeregion. The inventive catheter may include a balloon. The catheter mayhave a shaft of varying flexibility which contains several lumen. Theinner, or delivery, lumen generally may be used with a guide wire toaccess target sites within the body through the flexible, small diametervessels of the body. The delivery lumen may be also used for placementof occlusive materials, e.g., in an aneurysm. Inflation of the optionalmicro-balloon, located near the distal tip of the catheter, is effectedusing the inflation lumen. The push/pull wire tubing contains a wire,which when manipulated, flexes the catheter's distal tip.

BACKGROUND OF THE INVENTION

Endovascular therapy has been used to treat different conditions, suchtreatments including control of internal bleeding, occlusion of bloodsupply to tumors, and occlusion of aneurysm. Often the target site ofthe malady is difficult to reach. Because of their ability to accessremote regions of the human body and deliver diagnostic or therapeuticagents, catheters are increasingly becoming components of endovasculartherapies. Vascular catheters may be introduced into large arteries,such as those in the groin or in the neck, and then pass throughnarrowing regions of the arterial system until the catheter's distal tipreaches the selected delivery site. To be properly utilized, cathetersare often stiffer at their proximal end to allow the pushing andmanipulation of the catheter as it progresses through the body butsufficiently flexible at the distal end to allow passage of the cathetertip through the body's blood vessels without causing significant traumato the vessel or surrounding tissue.

Microcatheters, such as those shown in U.S. Pat. Nos. 4,884,579 and4,739, 768, each to Engleson, allow navigation through the body'stortuous vasculature to access such remote sites as the liver and thearteries of the brain. Although other methods of causing a catheter toproceed through the human vasculature exist (e.g., flow directedcatheters), a guidewire-aided catheter is considered to be both quickerand more accurate than other procedures. Catheters with deflectable orvariable stiffness distal ends (which increase the flexibility of thecatheter's distal end) have been disclosed in U.S. Pat. No. 6,083,222,to Klein et al; U.S. Pat. No. 4,983,169, to Furukawa; U.S. Pat. No.5,499,973, Saab; and U.S. Pat. No. 5,911,715, to Berg et al.

The addition of a fluid-expandable balloon on the distal end of thecatheter and a coupler on the proximal end allows various percutaneousmedical treatments such as pressure monitoring, cardiac output and flowmonitoring, angioplasty, artificial vaso-occlusion, and cardiac support.Balloon catheters generally include a lumen that extends from theproximal end and provides fluid to the balloon for inflation. Examplesof balloon catheters are disclosed in U.S. Pat. No. 4,813,934 toEngleson et al and U.S. Pat. No. 5, 437,632 to Engelson et al. A ballooncatheter with an adjustable shaft is shown in U.S. Pat. No. 5,968,012,to Ren et al.

For certain vascular malformations and aneurysms, it may be desirable tocreate an endovascular occlusion at the treatment site. A catheter istypically used to place a vaso-occlusive device or agent within thevasculature of the body either to block the flow of blood through avessel by forming an embolus or to form such an embolus within ananeurysm stemming from the vessel. Formation of an embolus may alsoinvolve the injection of a fluid embolic agent such as microfibrillarcollagen, Silastic beads, or polymeric resins such as cyanoacrylate.Ideally, the embolizing agent adapts itself to the irregular shape ofthe internal walls of the malformation or aneurysm. Inadvertent embolismdue to an inability to contain the fluid agent within the aneurysm isone risk which may occur when using fluid embolic agents.

Mechanical vaso-occlusive devices may also be used for embolusformation. A commonly used vaso-occlusive device is a wire coil or braidwhich may be introduced through a delivery catheter in a stretchedlinear form and which assumes an irregular shape upon discharge of thedevice from the end of the catheter to fill an open space such as ananeurysm. U.S. Pat. No. 4,994,069, to Ritchart et al, discloses aflexible, preferably coiled, wire for use in a small vesselvaso-occlusion.

Some embolic coils are subject to the same placement risks as that offluid embolic agents in that it is difficult to contain the occlusivecoil within the open space of the aneurysm. A need exists for a deliverysystem which accurately places the occluding coil or fluid and ensuresthat the occluding coil or fluid does not migrate from the open spacewithin the aneurysm. The delivery catheter must have a small diameter,have a highly flexible construction which permits movement along asmall-diameter, tortuous vessel path, have a flexible method ofplacement to ensure accuracy, and must have a method to prevent coil orembolizing agent leakage.

SUMMARY OF THE INVENTION

This invention is a catheter or catheter section. Although it desirablyhas a balloon region located from distal of an inflatable member toproximal of that inflatable member, where the inflatable member iswithin the balloon region, it need not have a balloon region or aninflatable member. The inventive catheter has a flexible joint regionlocated generally in the distal area of the catheter, often within thatballoon region. The catheter includes a wire configured to flex theflexible joint region. Where the catheter includes an inflatable member,the flexible joint may variously be distal of the inflatable member,within the inflatable member, or proximal of the inflatable member. Theflexible joint region preferably has a flexibility of up to about 90°.The flexible joint region, because the catheter wire may be too rigid,may also be manipulatable in a circular direction relative to the axisof the catheter.

The wire may be slidingly held, e.g., within a separate tubing. Thistubing may potentially be used to aid in adjusting the flexibility ofthe joint region. This may be accomplished by several differentvariations. One variation utilizes a wire tubing having collinearconsecutive sections of decreasing wall thickness. Alternatively, thewire tubing may be tapered according to the desired degree of jointflexibility. The tubing itself may be a braided tubing which may be ofvarying flexibility.

The flexible joint itself may be, for instance, a coil member, perhapshaving a section with a pitch which is larger than adjacent coilpitches. The flexible joint may instead be a braid, perhaps with asection with a pic which is larger than the pic of one or more adjacentsections. The flexible joint may also be made up of a polymer tubingwith a section which is softer than adjacent tubing polymers or a regionhaving a wall thickness that is thinner than adjacent wall thickness.

In taking advantage of the flexibility and capabilities of the presentinvention, a variation capable of twisting in a helical orcorkscrew-like manner may be accomplished with or without an inflatablemember or balloon region. This variation is particularly useful intraversing tortuous vasculature and in making difficult approaches toaneurysms. This alternative varation utilizes a wire which may be woundabout the guidewire or inner tubing and fixedly attached. It is thuspossible to wind the wire any number of times or just a few degrees offthe wire axis depending upon the vasculature being traversed and thedegree of flexibility or twisting desired. Moreover, differentvariations may be developed capable of twisting in a left or righthanded orientation.

The present invention may also incorporate various rapid exchangevariations.

The inflatable member or balloon may be of a material selected from thegroup consisting of elastomers such as silicone rubber, latex rubber,natural rubber, butadiene-based co-polymer, EPDM, and polyvinyl chlorideor thermoplastic polymers such as polyethylene, polypropylene, andnylon.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A, 1B, and 1C are external views of several variations of theinventive catheter device.

FIG. 2A depicts a cross sectional view of a proximally placed hingeregion a variation of the distal region of the inventive catheter.

FIG. 2B depicts a cross sectional view of a mid-balloon hinge regionplacement for a variation of the distal region of the inventivecatheter.

FIG. 2C depicts a cross sectional view of a distally placed hinge regionin a variation of the distal region of the inventive catheter.

FIG. 2D depicts a cross sectional view of an additional mid-balloonhinge region placement for one variation of the distal region of theinventive catheter.

FIG. 3A depicts a cross-sectional view of an alternate hinge regionconstruction for the distal region of the inventive catheter. The hingeregion of FIG. 3A is composed of a section of material which issurrounded by regions of greater stiffness.

FIG. 3B depicts a cross-sectional view of an alternate hinge regionconstruction for the distal region of the inventive catheter. The hingeregion of FIG. 3B is composed of a coil of varying pitch.

FIG. 3C depicts a cross-sectional view of an alternate hingeconstruction for the distal region of the inventive catheter. The hingeof FIG. 3C is composed of a region of thinned tubing wall surrounded byregions of thickened tubing wall.

FIG. 3D depicts a cross-sectional view of an alternate hinge regionconstruction for the distal region of the inventive catheter. The hingeregion of FIG. 3B is composed of a braided region which is flanked byregions of higher braid density.

FIGS. 4A-4H are cross-sectional views of catheter shafts displaying thevarious relative positions of the push/pull wire lumen, inflation lumen,and delivery lumen.

FIG. 5 depicts the positions of the radio-opaque markers positionedwithin the distal end of the catheter tip.

FIG. 6A depicts the relative position of the distal end of the cathetertip when not flexed.

FIG. 6B depicts the relative position of the distal end of the catheterwhen flexed by pulling the push/pull motion wire.

FIG. 6C depicts the relative position of the distal end of the catheterwhen flexed by pushing the push/pull motion wire.

FIG. 7A depicts a variation having a push/pull wire tubing withconsecutively smaller cross-sections.

FIG. 7B depicts an alternative variation having a tapering push/pullwire tubing.

FIG. 7C depicts a cross-sectional view of the sectioned push/pull wiretubing from FIG. 7A.

FIG. 7D depicts a cross-sectional view of the tapered push/pull wiretubing from FIG. 7B.

FIG. 8A depicts a variation where the push/pull wire may be partiallywound about the guidewire tubing.

FIG. 8B depicts a cross-section of FIG. 8A where the push/pull wire iswound in a right-handed orientation.

FIG. 8C depicts a cross-section of FIG. 8A with an alternative variationwhere the push/pull wire is wound in a left-handed orientation.

FIG. 9 depicts a variation having a catheter tip which may be rotated bya twisting push/pull wire.

FIGS. 10A, 10B, and 10C are external views of several variations of theinventive catheter device incorporating a rapid exchange variation.

FIGS. 11A, 11B, 11C, and 11D depict the steps of using the inventivecatheter by respectively inserting the distal end of the inventivecatheter into a blood vessel, placing a vaso-occlusive device within ananeurysm, and removing of the catheter.

DETAILED DESCRIPTION OF THE INVENTION

This invention involves a multi-lumen, catheter having a manipulatabledistal tip and is for the delivery of vaso-occlusive materials orimplants. The inventive catheter may include one or more distally placedballoon members. The device is shown in detail in the Figures whereinlike numerals indicate like elements. The catheter preferably includes ashapeable, flexible distal section. The flexible section, or “hingeregion”, preferably is manipulated from outside the body during theprocess of delivering the verso-occlusive device or material. The terms“hinge region”, “hinge”, or “flexible joint” may be used interchangeablyfor our applications.

FIG. 1A shows a catheter assembly 23 made according to one variation ofthe invention. This variation of the catheter assembly 23 includes acatheter shaft 25 comprised of a flexible, thin walled body or tube 26having an inner lumen which extends between proximal and distal catheterends 24, 37, respectively. The tube 26 is preferably a generallynondistensible polymer having the appropriate mechanical properties forthis application, and preferably polyethylene (e.g., HDPE, LDPE, LLDPE,MDPE, etc.), polyesters (such as Nylon), polypropylene, polyimide,polyvinyl chloride, ethylvinylacetate, polyethylene terephthalate,polyurethane (e.g. Texin such as that made by Bayer Corporation), PEBAX,fluoropolymers, mixtures of the aforementioned polymers, and their blockor random co-polymers.

This variation of the inventive catheter assembly generally has severaloverall functions: a.) access through the vasculature to the brain (orother vascular site) often, but not necessarily, using a guide wire; b.)inflation of the inflatable member or balloon to close or to restrict anartery or the mouth of an aneurysm prior to or during placement of avaso-occlusive device, thereby requiring a fluid pathway for inflationof the inflatable member; c.) flexion of a “hinge region” in theneighborhood of the distal end of the catheter by a wire extendingproximally through the catheter; and d.) introduction of avaso-occlusive device or material for eventual placement in thevasculature, thereby requiring a pathway or storage region for thevaso-occlusive device. These functions may be achieved by features foundat the proximal and distal regions of the catheter.

The proximal catheter end 24 may be provided with a fitting 18 (e.g., a“LuerLok”) through which fluid may be supplied to the catheter'sinflation lumen through a side port 16. The proximal end of the catheteris provided with a second port 20 and a fitting 22 through which apush/pull wire may be used to manipulate the hinge region 32 in thedistal catheter tip. The proximal end fitting 18 includes an axiallyextending port 14 which communicates with the catheter's delivery/guidewire lumen. The optional guide wire 12 may have any suitableconstruction for guiding the flexible catheter to its intended sitewithin the body. The proximal end of the guide-wire 12 may be equippedwith a handle 10 for applying torque to the guide wire 12 duringcatheter operation. The guide-wire may have a variable stiffness orstepped diameter along its length which typically, e.g., alarger-diameter, stiffer proximal region and one or moresmaller-diameter, more flexible distal regions.

The distal portion 35 of the catheter is made of an inflatable member30, typically a balloon, a hinge region 32, and an opening or aperture36 for delivery of the vaso-occlusive device or material. This opening36 may also be used for delivery of drugs and the vaso-occlusive deviceto the selected vascular site. The distal end region 35 of the catheter25 is provided with an inflatable balloon 30 which, when inflated, aidsin the placement of vaso-occlusive materials or devices by blocking theentrance to the aneurysm or the artery adjacent to the aneurysm.

The balloon wall section (discussed in greater detail below) ispreferably formed from a thin sleeve of polymeric material and attachedat its opposite sleeve ends to a relatively more rigid tube section.FIGS. 1A, 1B, and 1C display various configurations of the distalcatheter tip 35 positioning based on the placement of the flexible hingeregion. FIGS. 1A, 1B, and 1C respectively show variations of theinventive catheter 23 in which the hinge region 32 is placed proximal to(FIG. 1A), within (FIG. 1B), and distal to (FIG. 1C) the inflatablemember region 30. Flexion of the hinge region is achieved through remotemanipulation of the push/pull wire 21.

FIGS. 2A through 2D illustrate variations of the distal end region 35and hinge region 32 of the catheter illustrated in FIG. 1A, 1B, and 1C.

The catheter tube 40 of FIG. 2A has an inflatable member 44, preferablya balloon, which is formed by an inflatable sleeve secured at its ends41, 43 to the catheter tube wall 40. The inflatable member or balloon 44may be of a shape, thickness, and material as is typical of balloonsused in neurovascular balloon catheters. Preferably, though, theinflatable member or balloon 44 is formed of a thin polymeric material,and preferably an elastomeric, stretchable material such as siliconerubber, latex rubber, polyvinyl chloride, complex co-polymers such asstyrene-ethylene butylene-styrene copolymers such as C-FLEX, oralternatively, a non-stretchable film material such as polyethylene,polypropylene, or polyamides such as Nylon. Attachment of the sleeveends to the catheter tube may be by gluing, heat shrinkage, mechanicalfastener, or other suitable method. The inflation lumen 42 allowscommunication between the inflation fluid source and the balloon 44through at least one opening 50 formed in the catheter tube 40.Inflation and deflation of the balloon are effected by the passage ofradio-opaque fluid, saline, or other fluid. The push/pull wire tubing 60extends throughout the catheter tube 40 and protects the passage of thepush/pull wire 62 which is connected to the inner wall of the cathetertube 40. To assist in preventing collapse of the tube 60 enclosing thepush/pull wire 62 and to prevent kinking or bulging during actuation,the push/pull wire tubing 60 may have additional structure preferablyprovided by a layer of higher stiffness polymer (e.g., a polyimide), asupport coil, or a support braid.

Axial manipulation of the push/pull wire 62 via the proximal wire port(20 in FIG. 1A) allows flexion of the distal end 35 of the catheter (25in FIG. 1A). The guide wire 57 extends through the delivery lumen 55which lies interior to the catheter tube 40. The push/pull wire 62extends through the push/pull wire tubing 60 and may be bonded to theradio-opaque band 67 which surrounds the catheter's distal end 65.Radio-opaque bands may be made of any number of conventionalradio-opaque materials, e.g., platinum. The hinge region 58 at which thedistal catheter tip 65 flexes due to proximal manipulation of thepush/pull wire 62 may be located proximal to, within, or distal to theballoon, as displayed respectively in FIGS. 2A, 2B, and 2C.

As shown in FIG. 2A, when the hinge region 58 is placed proximally ofthe balloon 44, the push pull wire tubing 60 extends to a region whichis proximal of the distal end of the balloon 44 to allow flexion of theregion of the catheter's distal end 65 which includes the entire balloon44. If the hinge region 58 is placed interior to the balloon, as in FIG.2B, flexion of the catheter's distal end 65 occurs such that the pointof flexion is within the balloon (also displayed in FIG. 1B). FIG. 2Cshows the placement of hinge 58 distal to the balloon; flexion duringdistal-hinge placement occurs such that the manipulatable region of thecatheter's distal end 65 does not include any portion of the balloon 44.

FIG. 2D shows placement of the hinge region 58 interior to the balloon44. The balloon 44 extends between the guidewire/delivery tube 56 andthe outer catheter tube 40 enclosing the annular inflation lumen 42. Thepush/pull wire 62 is attached to the distal end 65 of theguidewire/delivery tube 56.

In each of the variations shown in FIGS. 2A, 2B, 2C, and 2D, thepush/pull wire 62 is distally attached to a radio-opaque band 67.Although this is a preferred variation, other attachment sites forattachment of the push/pull wire 62 distal to the hinge region 58 willbe apparent.

The hinge region may be made up of any material or structuralconfiguration which allows flexion based on remote manipulation bymovement of the push/pull wire 62. Several variations of preferredconfiguration are shown in FIGS. 2D, 3A, 3B, and 3C.

In FIG. 2D, extension of the delivery tube 56 beyond the end of theinflation lumen 42 allows remote manipulation of the catheter's distalend 65 if the push/pull wire 62 is attached to a marker or platinum band67 which is located distal to the end of the inflation lumen. In thisconfiguration, remote manipulation of the push/pull wire allows flexionto occur between the end of the inflation lumen 42 and the marker 67 towhich the push/pull wire 62 is attached. The delivery tube 56 may bemade of any of the materials listed above with respect to tube 26 inFIG. 1.

FIG. 3A displays a cross section of the catheter 70 wall. The hingesection of FIG. 3A is made from contiguous regions of tubing where onesection of the catheter wall 77 is made from a material with a stiffnesswhich is less than the stiffness of the material of the flankingsections of catheter wall 75, 79. These regions of tubing are preferablymade through extrusion, by doping, or heat treating a region of thetubing.

FIG. 3B displays a hinge region 88 which utilizes a coil 90 of varyingpitch imbedded in the catheter wall. Because the variation in pitch ofthe coil 90 produces regions of varying flexibility, the lower pitchregion 88 is more flexible than the region of higher pitch 89. Thehigher pitch region 89 is stiffer during manipulation of the push/pullwire 86.

As shown in FIG. 3C, if a thinned region of catheter wall 105 is flankedby regions of greater wall cross-sectional area 100, 108, the section108 of the catheter wall which is distal to the thinned section 105 willact as a hinge when the distal end of the catheter is manipulated usingthe push/pull wire 96. The variations in wall cross sectional area maypreferably be created during an extrusion process.

FIG. 3D displays a hinge which utilizes a braided ribbon 94 with varyingbraid pitch, that is embedded between outer 101 and inner 103 layers ofthe catheter wall. The variation in pitch of the braided ribbon 105produces regions of varying flexibility. If a region of lower braidpitch 92 is flanked by regions of higher braid pitch 90, the region ofgreater pitch 89 is stiffer during manipulation of the distal cathetertip. The braid 94 is preferably made from a number of metallic ribbonsor wires which are members of a class of alloys known as super-elasticalloys, but may also be made from other appropriate materials such asstainless steel or polymers such as liquid crystal polymers (LCP's).Preferred super-elastic alloys include the class of titanium/nickelmaterials known as nitinol. Additional treatment to the braid prior toassembly, such as heat-treatment, may be required or desired to preventbraid unraveling, changes in diameter, or spacing during handling. Thebraids which may be utilized in this invention are preferably made usingcommercially available tubular braiders. The term “braid” is meant toinclude tubular constructions in which the ribbons making up theconstruction are woven radially in and in-and-out fashion as they crossto form a tubular member defining a single lumen. The braid ispreferably made from a suitable number of ribbons or wires.

Some of the various configurations of the catheter's lumina (inflation,push/pull, and delivery) are displayed in FIGS. 4A through 4H. In FIG.4A, the inflation lumen 122 and push/pull wire lumen 124 are formedinterior to the catheter wall 120, while the interior catheter wallforms the guide wire lumen 128. In FIG. 4B, the catheter wall 120 formsthe guide wire lumen 128 which contains the inflation lumen 122 andpush/pull wire lumen 124. The inflation lumen 122 is formed interior tothe catheter wall 120 of FIG. 4C, while the push/pull wire lumen 124lies within the larger coil lumen 128 (which is formed by the catheterwall 120). FIG. 4D is a variation of FIG. 4C in which the push/pull wirelumen 124 lies interior to the catheter wall 128 while the inflationlumen 122 lies within the larger coil lumen 128. In FIG. 4E, theinterior catheter wall 120 forms the inflation lumen 122, and thepush/pull wire lumen 124 and the guide wire lumen 128 are found withinthe inflation lumen 122. The inflation lumen 122 surrounds the guidewire lumen 128 and lies within the region formed interior catheter wall120 in FIG. 4F, while the push/pull wire lumen 124 lies within thecatheter wall 120. In FIG. 4G, one shared lumen 123 serves as thepush/pull and inflation lumen; the shared push/pull and inflation lumen123 along with the guide wire lumen 128 lie within the catheter wall120. Another alternate variation of the lumina positioning, shown inFIG. 4H, has the push/pull wire lumen 124 lying interior to theinflation lumen 122 which is contained within the catheter wall 120,while a separate lumina for the guide wire 128 also is contained withinthe catheter wall.

The tube constructions, hinge region construction, and other tubingforming the various lumina discussed herein may be created throughextrusion, sequential production (in which the parts are manufacturedseparately and later assembled together), or some other method.

As displayed in FIG. 5, another variation of the present invention mayinvolve the addition of radio-opaque markers 190. The lengthened distalsection 200 may be provided with a number of spaced radio-opaque markers190, 191, 192, and 193. Balloon markers 195, 196 may be provided toindicate the position of the balloon during the vascular procedure. Themarkers may be spaced, for instance, such that the inter-marker distancecorresponds to the length of the coil to be delivered. Markers 195, 196may be spaced apart by a known or predetermined distance, e.g., 3 cm,both proximally and distally of the balloon member. Also, the variousmarkers, particularly those located adjacent the balloon member, may bedisposed outside the balloon member, as depicted, or optionally inside.

FIGS. 6A, 6B, and 6C show the operation of the inventive flexible distalcatheter tip.

In FIG. 6A, the remotely-manipulatable distal end 136 extends beyond thehinge 135 and allows greater access to the delivery site of thevaso-occlusive member 137 during surgical procedures. Manipulation ofthe push/pull wire 143 allows flexion of the catheter distal tip 136.

If the push/pull wire 143 is pushed or axially manipuliated, as shown inFIG. 6B, the distal tip 145 is flexed upward through an angle determinedby the pressure applied to the push/pull wire. Generally, the deflectionangle of the catheter 140 as the push/pull wire 143 is pushed mayapproach up to about 90° in one direction.

If the push/pull wire 143 is pulled as in FIG. 6C, rotation from theun-manipulated position through an angle up to about 90° opposite thedirection shown in FIG. 6B is initiated; again, this angle is in adirection which is opposite to that of the pull-manipulation butgenerally in the same plane. The push/pull wire 143 extends through outthe push/pull wire lumen 141 and may be bonded to the radio-opaque band142 found at the distal end 145 of the catheter 140 tip.

FIG. 7A depicts an alternative variation 210 which is similar to thatshown in FIG. 2D. The tubing 56 itself may be a braided tubing which maybe of varying flexibility. However, variation 210 depicts a push/pullwire tubing 212 having a stepped distal end 213. Stepped push/pull wiretubing 212 may be comprised of similar materials and structures aspush/pull wire tubing 60 but having a series of successively decreasingcross-sectional areas on stepped distal end 213. The number ofsuccessively decreasing cross-sections and the associated lengths ofeach decreased section may vary depending upon the degree of flexibilitynecessary or desired within catheter distal end 65. Moreover, variation210 depicts stepped distal end 213 extending into inflatable member 44;however, the relative positioning of stepped push/pull wire tubing 212to inflatable member 44 may be altered again depending on the desiredflexibility of catheter 40. Push/pull tubing 212 may itself be a braidedtubing which may be of varying flexibility. Also, the figure depictspush/pull wire tubing 212 as a separate tube, but it may also be in anyof the variational cross-sections discussed herein having the push/pullwire tubing 212 disposed, e.g., within the tubing and any braiding orcoils, or disposed exteriorly of any braiding or coils.

FIG. 7C depicts the cross-sectional view of the stepped push/pull wiretubing 212 from FIG. 7A. Tubing 212 may be attached or held to tubing 56by any of the various methods discussed herein, e.g., shrink-wrap. Thefigure depicts tubing 212 with three sections for illustrative purposesand tubing 212 may comprise any number of sections with variablethickness depending upon the degree of flexibility necessary or desired.

FIG. 7B depicts an additional alternative variation 214 which is similarto variation 210. However, variation 214 depicts push/pull wire tubing216 having a tapering distal end 217. Here, the degree of tapering maybe varied depending upon the degree of flexibility necessary or desired,as above.

FIG. 7D depicts the cross-sectional view of the tapered push/pull tubing216 from FIG. 7B. Tubing 216 may also be attached or held to tubing 56by any of the various methods discussed herein, e.g., shrink-wrap.Tubing 216 may be made to have any degree of tapering again dependingupon the degree of flexibility necessary or desired.

FIG. 8A depicts another variation 218 which enables a user to not onlymanipulate catheter distal end 65 within generally one plane, but alsoto manipulate or to twist catheter distal end 65, e.g., in a helical orcorkscrew-like manner. As illustrated, push/pull wire 62 emerges frompush/pull wire tubing 60 and may be rotated about guidewire/deliverytube 56 for attachment to an attachment point, e.g., radio-opaque band67 as shown, at some point not on the axis with the tubing 60. Insteadit may be attached preferably on an opposite side from where push/pullwire 62 emerges. The attachment point is preferably located distallyfrom push/pull wire tubing 60, but may vary depending upon the degree oftorque desired. Also, attachment of push/pull wire 62 along radio-opaqueband 67 may also vary depending upon the desired range of torquing ortwisting of catheter distal end 65. For example, push/pull wire 62 maybe placed along, e.g., radio-opaque band 67, in any location rangingfrom about 0° where little or no twisting occurs and up to about 180°where full rotation of catheter distal end 65 occurs about alongitudinal axis defined by catheter tube 40 and guidewire/deliverytube 56. At about 0°, push/pull wire 62 is attached to radio-opaque band67 at a point in aposition to where wire 62 emerges from tubing 60. Atabout 180°, as depicted in FIG. 8A, push/pull wire 62 is attached toradio-opaque band 67 at a point on an opposite side ofguidewire/delivery tube 56 from where wire 62 emerges.

In variation 218, push/pull wire tubing 60 may be held relative toguidewire/delivery tube 56 by any conventional shrink-wrap material 220or by any number of fastening methods discussed herein. Moreover, anynumber of cross-sectional arrangements described herein forguidewire/delivery tube 56 and push/pull wire tubing 60 may be utilizedas well. Also, the arrangement of variation 218 for wire 62 may beutilized with or without inflatable balloon member 44 and is shown inFIG. 9 without balloon member 44.

Although FIG. 8A depicts push/pull wire 62 wrapped half-way aroundguidewire/delivery tube 56, push/pull wire 62 may be wrapped any numberof times around tube 56 before being attached at a desired location onradio-opaque band 67.

FIG. 8B shows section A-A from FIG. 8A depicting push/pull wire 62wrapped in a right-handed orientation about guidewire/delivery tube 56.Wire 62 may alternatively be wrapped in a left-handed orientation aboutguidewire/delivery tube 56, as shown in FIG. 8C, which depicts the samecross-section of FIG. 8B.

In wrapping push/pull wire 62 about tube 56, manipulation of catheterdistal end 65 forces wire 62 to not only undergo tensile and compressiveforces along its longitudinal axis, but also torquing forces about itsaxis. FIG. 9 depicts variation 221 without a balloon member.Alternatively, the inventive catheter design also allows twisting of thecatheter tip without having to attach push/pull wire 62 along band 67 atvariable positions. This may be accomplished by utilizing open area 222,the area without push/pull wire tubing 60, and the stiffness of wire 62.Wire 62 may be torqued or twisted about its own axis at its proximal endby a user to bring about a rotation of the distal end of wire 62 and, inturn, catheter distal end 65. The degree of torquing or twisting ofcatheter distal end 65 may be controlled not only by the choice ofcatheter tubing materials, as discussed herein, but also by the lengthof open area 222 as well as by the choice of material and desiredstiffness of wire 62. This variation may allow a catheter having acombined ability to not only be pushed and pulled in a single plane, butto also be twisted in a helical or corkscrew-like manner, if desired.Although FIG. 9 depicts this variation without a balloon member, it maybe used with one as described in the other variations herein. Any numberof materials having sufficient strength and elasticity may be used forwire 62. Some materials which may be used include stainless steels,titanium, superelastic alloys (e.g., nitinol), or any of theircombinations and alloys.

As depicted in the Figures, particularly FIGS. 7A-7B and 8A-8C,radio-opaque bands 67 may optionally be used in conjunction with thedifferent variations as marking known or predetermined distances betweenthe bands 67, as discussed above.

FIG. 10A depicts variation 230 of the present invention which mayincorporate rapid exchange catheter apparatus and methods. A typicalrapid exchange catheter is described in detail in U.S. Pat. No.4,748,982 entitled “Reinforced Balloon Dilatation Catheter with SlittedExchange Sleeve and Method” by Horzewski et al., which is hereinincorporated by reference in its entirety. In this variation 230, theapparatus and methods of the present invention, as described herein, maybe used with guidewire 12. Rather than having guidewire 12 inserted fromthe proximal end of the catheter, guidewire 12 may instead be insertedthrough entry 232, which may be located along catheter 25 at apredetermined location proximal of distal end 35. This variation 230 mayfacilitate rapid exchanges of the inventive catheter assembly from abody lumen with other catheters, as desired by the operator.

FIGS. 10B and 10C depict entry 232 and insertable guidewire 12 used inconjunction with the manipulatable balloon catheter.

A remotely flexible distal tip is particularly useful when treating ananeurysm by placement of a vaso-occlusive device or material in theaneurysm. FIGS. 11A-11D depict such a placement.

FIG. 11A displays an inventive catheter 156 that has its distal endpositioned outside the mouth of an aneurysm 149 to deliver avaso-occlusive coil. The device is positioned using a guidewire 159.

Introduction of the catheter's distal end 165 into the aneurysm neck147, shown in FIG. 11B, displays the advantages of the inventiveremotely manipulatable catheter. Flexion of the catheter's distal tipusing the push/pull wire allows for greater maneuverability whenaccessing the aneurysm neck and aneurysm sac. The push/pull wire systemallows the distal end to be positioned as desired during the procedure,instead of before the procedure begins. Once the distal tip 165 has beenproperly positioned in the aneurysm neck 147, inflation of the balloon157 is then commenced to occlude the aneurysm neck 147, as shown in FIG.1C. Full occlusion of the aneurysm neck is desirable to ensure that thecoils 175 do not escape into the vessel when the coils are dischargedinto the aneurysm sac 149. Once the coil or coils 175 have beencompletely discharged 180 into the aneurysm sac 149, deflation of theballoon 157 allows retraction of the catheter's distal end 165 from theaneurysm (shown in FIG. 11D).

The applications of the inventive catheter discussed above are notlimited to the treatment of aneurysms, but may include any number ofvascular maladies. Modification of the above-described methods forcarrying out the invention, and variations of the mechanical aspects ofthe invention that are obvious to those of skill in the mechanical andguide wire and/or catheter arts are intended to be within the scope ofthe claims.

I claim:
 1. A catheter section, comprising: a balloon region comprisinga distal end and a proximal end and defining an axis therebetween; aninflatable member disposed in said balloon region; a flexible jointregion disposed within said balloon region; a tubing member furtherdisposed in said balloon region, said tubing member having a distal endand a proximal end and an axis therebetween, said tubing member having avariable wall thickness; and a wire configured to move said distal endabout said flexible joint region, said wire being disposed within saidtubing member.
 2. The catheter section of claim 1, wherein said tubingmember comprises a first wall thickness at a location proximal of saiddistal end and a second wall thickness at said distal end, said firstwall thickness being greater than said second wall thickness.
 3. Thecatheter section of claim 1, wherein said tubing member furthercomprises a plurality of consecutive tube sections, said tube sectionseach having a wall thickness less than an adjacent proximal tubesection.
 4. The catheter section of claim 1, wherein said tubing memberhas a tapered wall.